US11992486B2ActiveUtilityA1
Methods of treating prostate cancer
Est. expiryJul 29, 2036(~10 yrs left)· nominal 20-yr term from priority
A61P 35/04A61P 13/08A61P 35/00A61K 9/0053A61K 31/454
83
PatentIndex Score
0
Cited by
789
References
12
Claims
Abstract
Disclosed are methods of treating prostate cancer by administering niraparib to a human in need thereof.
Claims
exact text as granted — not AI-modifiedWe claim:
1. A method of treating prostate cancer in a human in need of such treatment comprising administering to the human a pharmaceutically acceptable amount of niraparib or a salt thereof, wherein the prostate cancer is antiandrogen resistant and wherein the human is carrying at least one DNA repair anomaly in a gene selected from the group consisting of BRCA-1 and BRCA-2.
2. The method of claim 1 , wherein the prostate cancer is castration-resistant prostate cancer.
3. The method of claim 1 , wherein the prostate cancer is metastatic castration- resistant prostate cancer.
4. The method of claim 1 , wherein niraparib or a salt thereof is administered in an amount of from about 30 mg niraparib/day to about 400 mg niraparib/day.
5. The method of claim 1 , wherein niraparib or a salt thereof is administered in an amount of about 300 mg niraparib/day.
6. The method of claim 5 , wherein niraparib or a salt thereof is administered orally, once daily, in 100 mg niraparib oral dosage forms.
7. The method of claim 1 , wherein the human has had at least one line of taxane-based chemotherapy.
8. The method of claim 1 , wherein the prostate cancer has been exposed to at least one line of enzalutamide-, apalutamide-, or abiraterone acetate-based antiandrogen therapy.
9. The method of claim 1 , wherein the DNA repair anomaly is a genomic lesion.
10. The method of claim 9 , wherein the genomic lesion is a homozygous deletion, heterozygous deletion plus deleterious mutation, or copy neutral loss of heterozygosity plus deleterious mutation.
11. The method of claim 1 , further comprising determining whether the human is carrying at least one DNA repair anomaly in a gene selected from the group consisting of BRCA-1 and BRCA-2.
12. A method of treating prostate cancer in a human in need of such treatment comprising:
determining whether the human is carrying at least one DNA repair anomaly in a gene selected from the group consisting of BRCA-1 and BRCA-2, and
administering to the human a pharmaceutically acceptable amount of niraparib or a salt thereof to a human who is carrying the at least one DNA repair anomaly,
wherein the prostate cancer is antiandrogen resistant.Join the waitlist — get patent alerts
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